HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ethanol → 4-(1-Benzyl-piperidin-4-ylidenemethyl)-benzonitrile
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Edukt | Diethyl (4-Cyanobenzyl)phosphonate | HCID 241438 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-(1-Benzyl-piperidin-4-ylidenemethyl)-benzonitrile | HCID 67435655 | 87,7% |
Reaktionsschritte
Under argon, to a stirred mixture of N-benzyl-4-piperidone (Aldrich) (26.0 g, 0.137 mol) and (4-cyano-benzyl)-phosphonic acid diethyl ester (36.6 g, 0.1445 mol) in dimethylformamide (260 mL) sodium hydride (60%, 7.8 g, 0.195 mol) was added at 0° C. The reaction mixture was stirred at room temperature overnight, then ethanol (10 mL) was added dropwise, the so obtained mixture was poured into water (300 mL), and extracted with diethyl ether (3×300 mL). The organic layer was dried over sodium sulfate and concentrated. The residue was purified by column chromatography using Kieselgel 60 (0.040-0.063 mm) (Merck) as adsorbent, and n-hexane:ethyl acetate=2:1 as eluent to yield 34.65 g (87%) of the title compound as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08034827B2 |
| Quelldatensatz | uspto-grants-2011_10 |
| ORD ID | ord-0e4b8fa593604101a6f0ea884a195f99 |
| Quellennotiz | uspto-grants-2011_10 |